Home
>
National Drug Code (NDC)
>
MINOCYCLINE HYDROCHLORIDE
MINOCYCLINE HYDROCHLORIDE - 68084-289-01 - (MINOCYCLINE HYDROCHLORIDE)
Drug Information of MINOCYCLINE HYDROCHLORIDE
| Product NDC: | 68084-289 |
| Proprietary Name: | MINOCYCLINE HYDROCHLORIDE |
| Non Proprietary Name: | MINOCYCLINE HYDROCHLORIDE |
| Active Ingredient(s): | 100 mg/1 & nbsp; MINOCYCLINE HYDROCHLORIDE |
| Administration Route(s): | ORAL |
| Dosage Form(s): | CAPSULE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of MINOCYCLINE HYDROCHLORIDE
| Product NDC: | 68084-289 |
| Labeler Name: | American Health Packaging |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA065005 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20080827 |
Package Information of MINOCYCLINE HYDROCHLORIDE
| Package NDC: | 68084-289-01 |
| Package Description: | 10 BLISTER PACK in 1 CARTON (68084-289-01) > 10 CAPSULE in 1 BLISTER PACK (68084-289-11) |
NDC Information of MINOCYCLINE HYDROCHLORIDE
| NDC Code | 68084-289-01 |
| Proprietary Name | MINOCYCLINE HYDROCHLORIDE |
| Package Description | 10 BLISTER PACK in 1 CARTON (68084-289-01) > 10 CAPSULE in 1 BLISTER PACK (68084-289-11) |
| Product NDC | 68084-289 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | MINOCYCLINE HYDROCHLORIDE |
| Dosage Form Name | CAPSULE |
| Route Name | ORAL |
| Start Marketing Date | 20080827 |
| Marketing Category Name | ANDA |
| Labeler Name | American Health Packaging |
| Substance Name | MINOCYCLINE HYDROCHLORIDE |
| Strength Number | 100 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Tetracycline-class Drug [EPC],Tetracyclines [Chemical/Ingredient] |
